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TAK-701 的初步测试(第 1 阶段),一种人源化肝细胞生长因子结合抗体,由儿科临床前测试计划进行。

Initial testing (Stage 1) of TAK-701, a humanized hepatocyte growth factor binding antibody, by the Pediatric Preclinical Testing Program.

机构信息

Nationwide Children's Hospital, Columbus, Ohio.

出版信息

Pediatr Blood Cancer. 2014 Feb;61(2):380-2. doi: 10.1002/pbc.24756. Epub 2013 Sep 9.

DOI:10.1002/pbc.24756
PMID:24019233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3961752/
Abstract

TAK-701 is a humanized antibody that binds hepatocyte growth factor (HGF), thus suppressing c-Met transduced signaling and c-Met dependent proliferation and migration of tumor cells. Six childhood solid tumor xenografts were selected for evaluating TAK-701 based on immunochemical detection of HGF/c-Met autocrine signaling [i.e., pMet(Tyr1349) and HGF positive]. TAK-701 was tested using a dose of 30 mg/kg administered by the intraperitoneal (IP) route twice weekly for 4 weeks. TAK-701 did not induce significant differences in EFS distribution in treated tumors compared to control tumors. Objective responses were not observed in any of the tested solid tumor xenografts.

摘要

TAK-701 是一种人源化抗体,可与肝细胞生长因子 (HGF) 结合,从而抑制 c-Met 转导信号以及肿瘤细胞的 c-Met 依赖性增殖和迁移。为了基于 HGF/c-Met 自分泌信号的免疫化学检测(即 pMet(Tyr1349) 和 HGF 阳性)评估 TAK-701,选择了 6 种儿童实体瘤异种移植物。使用 30mg/kg 的剂量通过腹腔 (IP) 途径每周两次给药 4 周来测试 TAK-701。与对照肿瘤相比,TAK-701 并未在治疗肿瘤中诱导 EFS 分布的显著差异。在任何测试的实体瘤异种移植物中均未观察到客观反应。

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